Docking and QSAR Studies of Aryl-valproic Acid Derivatives to Identify Antiproliferative Agents Targeting the HDAC8-Reference-Cited by-同舟云学术

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Docking and QSAR Studies of Aryl-valproic Acid Derivatives to Identify Antiproliferative Agents Targeting the HDAC8

Published:2017-06-19 Issue:7 Volume:17 Page:
ISSN:1871-5206
Container-title:Anti-Cancer Agents in Medicinal Chemistry
language:en
Short-container-title:ACAMC

Author:

Martínez-Pacheco Heidy,Ramírez-Galicia Guillermo,Vergara-Arias Midalia,Gertsch Jurg,Fragoso-Vazquez Jonathan Manuel,Mendez-Luna David,Abujamra A. L.,Cristina Cabrera-Perez Laura,Cecilia Rosales-Hernandez Martha,Mendoza-Lujambio I,Correa-Basurto Jose

Publisher

Bentham Science Publishers Ltd.

Subject

Cancer Research,Pharmacology,Molecular Medicine

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unveiling critical structural features for effective HDAC8 inhibition: a comprehensive study using quantitative read-across structure–activity relationship (q-RASAR) and pharmacophore modeling;Molecular Diversity;2024-06-13

2. Pathological Role of HDAC8: Cancer and Beyond;Cells;2022-10-09

3. Targeting Breast Cancer Cells with G4 PAMAM Dendrimers and Valproic Acid Derivative Complexes;Anti-Cancer Agents in Medicinal Chemistry;2020-10-27

4. Histone deacetylase 8 (HDAC8) and its inhibitors with selectivity to other isoforms: An overview;European Journal of Medicinal Chemistry;2019-02

5. Design of Drugs by Filtering Through ADMET, Physicochemical and Ligand-Target Flexibility Properties;Methods in Molecular Biology;2018

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